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Status |
Public on Oct 30, 2015 |
Title |
Comprehensive role of Zfp217 in m6A methylation [ChIP-seq] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Many transcriptional and epigenetic networks must be integrated to maintain self-renewal and pluripotency in embryonic stem cells (ESCs) and to enable induced pluripotent stem cell (iPSC) reprogramming. Here, we explore the role of Zfp217 as a key transcriptional factor in maintaining ES cell self-renewal by permorming genome-wide ChIP-Seq analyses.
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Overall design |
Examination of Zfp217 binding profiling by high throughput sequencing in mouse stem cells
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Contributor(s) |
Aguilo F, Zhang F, Zhang W, Walsh MJ |
Citation(s) |
26526723 |
Submission date |
Feb 06, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Martin J. Walsh |
E-mail(s) |
martin.walsh@mssm.edu
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Organization name |
Mount Sinai School of Medicine
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Department |
Structural and Chemical Biology
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Street address |
One Gustave L. Levy Pl.
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City |
New York |
State/province |
NY |
ZIP/Postal code |
10029 |
Country |
USA |
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Platforms (1) |
GPL9185 |
Illumina Genome Analyzer (Mus musculus) |
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Samples (2) |
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This SubSeries is part of SuperSeries: |
GSE65735 |
Comprehensive role of Zfp217 in m6A methylation |
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Relations |
BioProject |
PRJNA274813 |
SRA |
SRP053314 |